Editas Medicine to Present Pipeline and Platform Data Demonstrating Progress Towards Developing Transformative Gene Editing Medicines at the American Society of Gene and Cell Therapy Annual Meeting

Rhea-AI Summary

Editas Medicine (Nasdaq: EDIT) announced the acceptance of four abstracts, including three oral presentations, at the 25th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT) from May 16-19, 2022. Key presentations feature preclinical data on EDIT-202, safety results from the BRILLIANCE trial of EDIT-101, and findings on EDIT-103 for treating retinal diseases. The company aims to share significant updates on its innovative gene editing technologies, reinforcing its commitment to developing transformative therapies for serious conditions.

CAMBRIDGE, Mass., May 02, 2022 (GLOBE NEWSWIRE) -- Editas Medicine, Inc. (Nasdaq: EDIT), a leading genome editing company, today announced that four abstracts have been accepted for presentation, including three oral presentations, at the 25^th Annual Meeting of the American Society of Gene and Cell Therapy (ASGCT) being held in Washington, D.C., and virtually, May 16 – 19, 2022. The Company is presenting data on its pipeline and platform technologies to support ongoing development programs.

Key Editas Medicine presentations at ASGCT include:

• Preclinical data on EDIT-202 demonstrating maintained expression levels of CD16 and mbIL15, prolonged persistence in the absence of exogeneous cytokines and significantly enhanced anti-tumor efficacy in an in vivo solid tumor model.
• Safety data from the BRILLIANCE trial of EDIT-101 demonstrating a favorable immunogenic profile.
• Preclinical data from non-human primate studies of EDIT-103, in development for the treatment of rhodopsin-associated autosomal dominant retinitis pigmentosa (RHO-adRP), demonstrating nearly 100% gene editing knockout of endogenous RHO gene and more than 30% replacement protein levels.
• Data demonstrating SLEEK (SeLection by Essential-gene Exon Knock-in) gene editing is an optimal strategy for achieving robust multi-transgene knock-in for the next generation of cell therapy medicines.

“Editas Medicine is making strong progress towards the clinic with our preclinical pipeline and in our efforts to develop transformative medicines for people living with serious diseases, including ocular diseases, hemoglobinopathies, and cancer,” said Mark S. Shearman, Ph.D., Executive Vice President and Chief Scientific Officer, Editas Medicine. “We look forward to sharing compelling data and important updates for several of our programs, including EDIT-101, EDIT-103, EDIT-202, and our SLEEK gene editing method at ASGCT later this month.”

The complete list of Editas Medicine presentations is below. Abstracts can be accessed on the ASGCT website, and the presentations will be posted on the Editas Medicine website during the conference.

Oral Presentations:
Title: Exploratory Immuno-Safety Profile of EDIT-101, a First-in-Human In Vivo CRISPR Gene Editing Therapy for CEP290-Related Retinal Degeneration
Session Date and Time: Monday, May 16, 2022, 1:30 p.m. – 3:15 p.m. ET
Presentation Time: 2:45 p.m. – 3:00 p.m. ET
Session title: Gene and Cell Therapy Trials in Progress

Title: SLEEK: A Method for Highly Efficient Knock-in and Expression of Transgene Cargos for Next-generation Cell-based Medicines
Session Date and Time: Wednesday, May 18, 2022, 3:45 p.m. – 5:30 p.m. ET
Presentation Time: 5:00 p.m. – 5:15 p.m. ET
Session title: New Gene Editing Technologies and Applications

Title: A Mutation-Independent CRISPR/Cas9-Based ʻKnockout and Replaceʼ Strategy to Treat Rhodopsin-Associated Autosomal Dominant Retinitis Pigmentosa
Session Date and Time: Thursday May 19, 2022, 10:15 a.m. – 12:00 p.m. ET
Presentation Time: 10:15 a.m. – 10:30 a.m. ET
Session title: Ophthalmic and Auditory Diseases

Poster Presentation:
Title: EDIT-202, A Multiplexed CRISPR-Cas12a Gene-Edited iPSC-Derived NK Cell Therapy has Prolonged Persistence, Promotes High Cytotoxicity, and Enhances In Vivo Tumor Killing
Session Date and Time: Wednesday, May 18, 2022, 5:30 p.m. – 6:30 p.m. ET
Session Title: Cancer - Targeted Gene and Cell Therapy II

About Editas Medicine
As a leading genome editing company, Editas Medicine is focused on translating the power and potential of the CRISPR/Cas9 and CRISPR/Cas12a (also known as Cpf1) genome editing systems into a robust pipeline of treatments for people living with serious diseases around the world. Editas Medicine aims to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. For the latest information and scientific presentations, please visit www.editasmedicine.com.

Forward-Looking Statements
This press release contains forward-looking statements and information within the meaning of The Private Securities Litigation Reform Act of 1995. The words "anticipate," "believe," "continue," "could," "estimate," "expect," "intend," "may," "plan," "potential," "predict," "project," "target," "should," "would," and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. The Company may not actually achieve the plans, intentions, or expectations disclosed in these forward-looking statements, and you should not place undue reliance on these forward-looking statements. Actual results or events could differ materially from the plans, intentions and expectations disclosed in these forward-looking statements as a result of various factors, including: uncertainties inherent in the initiation and completion of preclinical studies and clinical trials and clinical development of the Company’s product candidates; availability and timing of results from preclinical studies and clinical trials; whether interim results from a clinical trial will be predictive of the final results of the trial or the results of future trials; expectations for regulatory approvals to conduct trials or to market products and availability of funding sufficient for the Company’s foreseeable and unforeseeable operating expenses and capital expenditure requirements. These and other risks are described in greater detail under the caption “Risk Factors” included in the Company’s most recent Annual Report on Form 10-K, which is on file with the Securities and Exchange Commission, and in other filings that the Company may make with the Securities and Exchange Commission in the future. Any forward-looking statements contained in this press release speak only as of the date hereof, and the Company expressly disclaims any obligation to update any forward-looking statements, whether because of new information, future events or otherwise.

FAQ

What are the key presentations by Editas Medicine at ASGCT 2022?

Editas Medicine's key presentations include data on EDIT-202's anti-tumor efficacy, safety data from the BRILLIANCE trial of EDIT-101, and preclinical findings for EDIT-103 targeting retinal diseases.

When will Editas Medicine present at the ASGCT conference?

Editas Medicine will present at the ASGCT conference from May 16-19, 2022, with specific oral presentations scheduled on May 16, 18, and 19.

What is EDIT-202's significance in cancer treatment?

EDIT-202 shows prolonged persistence and enhanced tumor killing in preclinical models, making it a promising candidate for cancer therapy.

What are the findings from the BRILLIANCE trial of EDIT-101?

The BRILLIANCE trial of EDIT-101 demonstrated a favorable immunogenic profile, indicating its potential safety in treating retinal degeneration.

How does the SLEEK gene editing method work?

SLEEK (SeLection by Essential-gene Exon Knock-in) is a novel gene editing technique by Editas Medicine, designed for robust multi-transgene knock-in to enhance cell-based therapies.